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Author:
Rafnar, Thorunn
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Genotype
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Single Nucleotide
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Author:
Rafnar, Thorunn
Topic:
Genotype
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Polymorphism
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Single Nucleotide
Search Results - Open Polar - "deCODE genetics"
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Discovery of common variants associated with low TSH levels and thyroid cancer r...
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A common variant at 8q24.21 is associated with renal cell cancer.
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A rare nonsynonymous sequence variant in C3 is associated with high risk of age-...
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Article in Journal/Newspaper
3
Author
Gudbjartsson, Daniel F
3
Kong, Augustine
3
Masson, Gisli
3
Rafnar, Thorunn
Stefansson, Kari
3
Sulem, Patrick
3
Thorsteinsdottir, Unnur
3
Gudmundsson, Julius
2
Helgadottir, Hafdis Th
2
Helgason, Hannes
2
Johannsdottir, Hrefna
2
Kiemeney, Lambertus A
2
Magnusson, Olafur Th
2
Mayordomo, Jose I
2
Panadero, Angeles
2
Stacey, Simon N
2
Thorleifsson, Gudmar
2
Walters, G Bragi
2
Aben, Katja K H
1
Aguillo, Esperanza
1
Bernstein, Paul S
1
Bjarnason, Hjordis
1
Bjornsdottir, Unnur S
1
Boon, Camiel J F
1
De Juan, Ana
1
Duan, Yaou
1
Duvvari, Maheswara R
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Einarsson, Gudmundur V
1
Eyjolfsson, Gudmundur I
1
Fauser, Sascha
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Topic
Genetic Predisposition to Disease
3
Genotype
Humans
3
Iceland
3
Polymorphism
Single Nucleotide
Genetic Variation
2
Genome-Wide Association Study
2
Human
2
Aged
1
Amino Acid Substitution
1
Base Sequence
1
Carcinoma
1
Chromosomes
1
Complement Activation
1
Complement C3
1
Complement C3b
1
Complement Factor H
1
Computational Biology
1
DNA
1
Erfðagreining
1
Erfðir
1
Frumurannsóknir
1
Gene Expression Regulation
1
Gene Frequency
1
Genetic Loci
1
Genome
1
Kidney Neoplasms
1
Krabbamein
1
Macular Degeneration
1
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Content Provider
Hirsla - Landspítali University Hospital research archive
3
Language
English
3
Open Polar Keyword
Iceland
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